Taller height and risk of coronary heart disease and cancer: A within-sibship Mendelian randomization study

Author:

Howe Laurence J123ORCID,Brumpton Ben345,Rasheed Humaira13ORCID,Åsvold Bjørn Olav36,Davey Smith George12ORCID,Davies Neil M123ORCID

Affiliation:

1. Medical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of Bristol

2. Population Health Sciences, Bristol Medical School, University of Bristol, Barley House, Oakfield Grove

3. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology

4. HUNT Research Center, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology

5. Clinic of Medicine, St. Olavs Hospital, Trondheim University Hospital

6. Department of Endocrinology, Clinic of Medicine, St. Olavs Hospital, Trondheim University Hospital

Abstract

Background:Taller people have a lower risk of coronary heart disease but a higher risk of many cancers. Mendelian randomization (MR) studies in unrelated individuals (population MR) have suggested that these relationships are potentially causal. However, population MR studies are sensitive to demography (population stratification, assortative mating) and familial (indirect genetic) effects.Methods:In this study, we performed within-sibship MR analyses using 78,988 siblings, a design robust against demography and indirect genetic effects of parents. For comparison, we also applied population MR and estimated associations with measured height.Results:Within-sibship MR estimated that 1 SD taller height lowers the odds of coronary heart disease by 14% (95% CI: 3–23%) but increases the odds of cancer by 18% (95% CI: 3–34%), highly consistent with population MR and height-disease association estimates. There was some evidence that taller height reduces systolic blood pressure and low-density lipoprotein cholesterol, which may mediate some of the protective effects of taller height on coronary heart disease risk.Conclusions:For the first time, we have demonstrated that the purported effects of height on adulthood disease risk are unlikely to be explained by demographic or familial factors, and so likely reflect an individual-level causal effect. Disentangling the mechanisms via which height affects disease risk may improve the understanding of the etiologies of atherosclerosis and carcinogenesis.Funding:This project was conducted by researchers at the MRC Integrative Epidemiology Unit (MC_UU_00011/1) and also supported by a Norwegian Research Council Grant number 295989.

Funder

Norwegian Research Council

MRC Integrative Epidemiology Unit

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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